Evidence map›Paper›PMID 26394043›Full record

ArticlePloS one2015

Magnetic Resonance Detection of CD34+ Cells from Umbilical Cord Blood Using a 19F Label.

Lucia E Duinhouwer, Bernard J M van Rossum, Sandra T van Tiel, Ramon M van der Werf, Gabriela N Doeswijk, Joost C Haeck, Elwin W J C Rombouts, Mariëtte N D Ter Borg, Gyula Kotek, Eric Braakman and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 24% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Transient loading of CD34International journal of nanomedicine · 2017
    Article
  6. Article
  7. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 1 institution in 1 country.

Lucia E DuinhouwerDepartment of Hematology, Erasmus University Medical Centre, Rotterdam, The Netherlands.
Bernard J M van RossumDepartment of Radiology, Erasmus University Medical Centre, Rotterdam, The Netherlands.
Sandra T van TielDepartment of Radiology, Erasmus University Medical Centre, Rotterdam, The Netherlands.
Ramon M van der WerfDepartment of Radiology, Erasmus University Medical Centre, Rotterdam, The Netherlands.
Gabriela N DoeswijkDepartment of Radiology, Erasmus University Medical Centre, Rotterdam, The Netherlands.
Joost C HaeckDepartment of Radiology, Erasmus University Medical Centre, Rotterdam, The Netherlands.
Elwin W J C RomboutsDepartment of Hematology, Erasmus University Medical Centre, Rotterdam, The Netherlands.
Mariëtte N D Ter BorgDepartment of Hematology, Erasmus University Medical Centre, Rotterdam, The Netherlands.
Gyula KotekDepartment of Radiology, Erasmus University Medical Centre, Rotterdam, The Netherlands.
Eric BraakmanDepartment of Hematology, Erasmus University Medical Centre, Rotterdam, The Netherlands.
Jan J CornelissenDepartment of Hematology, Erasmus University Medical Centre, Rotterdam, The Netherlands.
Monique R BernsenDepartment of Radiology, Erasmus University Medical Centre, Rotterdam, The Netherlands; Department of Nuclear Medicine, Erasmus University Medical Centre, Rotterdam, The Netherlands.
Erasmus University Rotterdam · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Impaired homing and delayed recovery upon hematopoietic stem cell transplantation (HSCT) with hematopoietic stem cells (HSC) derived from umbilical cord blood (UCB) is a major problem. Tracking transplanted cells in vivo will be helpful to detect impaired homing at an early stage and allows early interventions to improve engraftment and outcome after transplantation. In this study, we show sufficient intracellular labeling of UCB-derived CD34+ cells, with 19F-containing PLGA nanoparticles which were detectable with both flow cytometry and magnetic resonance spectroscopy (MRS). In addition, labeled CD34+ cells maintain their capacity to proliferate and differentiate, which is pivotal for successful engraftment after transplantation in vivo. These results set the stage for in vivo tracking experiments, through which the homing efficiency of transplanted cells can be studied.

Indexed as

Antigens, CD34Cells, CulturedCell TrackingColony-Forming Units AssayFetal BloodFlow CytometryFluorine RadioisotopesHematopoietic Stem CellsHumansLactic AcidMagnetic Resonance SpectroscopyMicroscopy, ConfocalNanoparticlesPolyglycolic AcidPolylactic Acid-Polyglycolic Acid CopolymerReproducibility of ResultsAntigens, CD34Fluorine RadioisotopesLactic AcidPolyglycolic AcidPolylactic Acid-Polyglycolic Acid Copolymer

Identifiers

PMID26394043
PMCPMC4578896
OpenAlexW2203269736

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.